Plh. Rinne et al., The shoot apical meristem restores its symplasmic organization during chilling-induced release from dormancy, PLANT J, 26(3), 2001, pp. 249-264
The shoot apex of overwintering perennials ceases its morphogenetic activit
y at the end of the growing season and transforms into a bud which is dorma
nt and freezing-tolerant, In birch (Betula pubescens) these events are trig
gered by short photoperiod, and involve the production of 1,3-beta -D-gluca
n containing sphincters on the plasmodesmata. As a result, all symplasmic p
athways shut down. Here we show that breakage of bud dormancy by chilling i
nvolves restoration of the symplasmic organization of the meristem. This re
storation is likely to be mediated by 1,3-beta -D-glucanase, which was pres
ent in small spherosome-like vacuoles that arose de novo during dormancy in
duction. During chilling these vacuoles were displaced from the bulk cytopl
asm to the cortical cytoplasm where they became aligned with the plasma mem
brane, often associated with plasmodesmata. At this stage the enzyme also a
ppeared outside the vacuoles. During chilling, 1,8-beta -D-glucan disappear
ed from the plasmodesmal channels and wall sleeves, and the plasmodesmata r
egained the capacity for cell-cell transport, as demonstrated by microinjec
tion of Lucifer Yellow CH and Fluorescein-tagged gibberellic acid. Collecti
vely, the present experiments demonstrate that restoration of the symplasmi
c organization of the meristem is indispensable for the release of buds fro
m dormancy and the assumption of a proliferation-competent state, and impli
cate 1,3-beta -D-glucanase action at the plasmodesmata. Based on these find
ings we propose a model for 'dormancy cycling' which depicts the meristem a
s passing through three sequential states of cellular communication with ch
aracteristic sensitivities to distinct environmental cues.